IL-36α and IL-36γ expressions in the differential diagnosis of palmoplantar psoriasis and palmoplantar eczema: A retrospective histopathologic and immunohistochemical study

J Cutan Pathol. 2022 Jan;49(1):42-48. doi: 10.1111/cup.14105. Epub 2021 Aug 8.

Abstract

Background: Diagnosing hyperkeratotic lesions on the palms and soles is often challenging for both clinicians and pathologists. Interleukin (IL)-36 cytokines play an important role in the pathogenesis of psoriasis.

Methods: We retrospectively re-evaluated hematoxylin-eosin-stained biopsy specimens of 30 patients with clinically diagnosed palmoplantar psoriasis (PP) and 30 patients with palmoplantar eczema (PE), and then performed IL-36α and IL-36γ immunohistochemistry.

Results: Among the histopathologic features, thinning of the rete ridges and vertical alternation of parakeratosis and orthokeratosis had the highest positive predictive value (PPV) in diagnosing PP (72.7% and 69.3%, respectively). Immunohistochemically, patients with PP predominantly showed diffuse or focal strong expression with IL-36α and IL-36γ staining in the upper layers of the epidermis (86.7% and 83.3%, respectively). The comparison of the mean IL-36α and IL-36γ expression scores significantly differed between PP and PE (P < .001). Among all histopathologic and immunohistochemical features, diffuse strong expression of IL-36α and IL-36γ staining had the highest PPVs in favor of a diagnosis of PP (75% and 76.7%, respectively).

Conclusions: Our data suggest that IL-36α and IL-36γ immunohistochemistry can be used in the differential diagnosis of PP and PE.

Keywords: IL-36α; IL-36γ; immunohistochemistry; palmoplantar eczema; palmoplantar psoriasis.

Publication types

  • Clinical Trial

MeSH terms

  • Adult
  • Diagnosis, Differential
  • Eczema* / diagnosis
  • Eczema* / metabolism
  • Eczema* / pathology
  • Female
  • Gene Expression Regulation*
  • Humans
  • Interleukin-1 / biosynthesis*
  • Male
  • Middle Aged
  • Psoriasis* / diagnosis
  • Psoriasis* / metabolism
  • Psoriasis* / pathology
  • Skin* / metabolism
  • Skin* / pathology

Substances

  • IL36A protein, human
  • IL36G protein, human
  • Interleukin-1